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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501345Generated: October 30, 2026

Cyclopropanecarbonyl chloride → tert-Butyl cyclopropanecarboxylate

https://huagongshe.com/reaction/501345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarbonyl chlorideHCID 77637—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
Producttert-Butyl cyclopropanecarboxylateHCID 13676038—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred suspension of 12.09 (107.1 mmol) of potassium t-butoxide in 200 mL ether at 0° C. under nitrogen was added 13.4 g (128.6 mmol) of cyclopropanecarboxylic acid chloride over 5 min. After 30 min at 0° C. the mixture was stirred at ambient temperature for an additional 30 min. The reaction mixture was poured into aqueous saturated sodium bicarbonate and extracted with ether. The organic layer was dried and carefully concentrated to deliver 15.0 g (99%) of a yellow oil as the desired ester product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772252B2
Source datasetuspto-grants-2010_08
ORD IDord-a1b727301538490faf6608fcdb945a36
Source noteuspto-grants-2010_08